1. 2024
  2. Tunable Approach to Diverse Phenethylamines via Reduction of 5-Aryloxazolidines with Triethylsilane

    Smorodina, A., Buev, E., Moshkin, V. & Sosnovskikh, V., 16 Feb 2024, In: Journal of Organic Chemistry. 89, 4, p. 2294-2305 12 p.

    Research output: Contribution to journalArticlepeer-review

  3. 2023
  4. Recyclization of 3,3-diacylpyrrolidines into pyrazolylethylamines: Pyrazole aromaticity vs pyrrolidine C - C bond

    Smorodina, A., Buev, E., Moshkin, V. & Sosnovskikh, V., 1 Dec 2023, In: Tetrahedron Letters. 133, 154830.

    Research output: Contribution to journalArticlepeer-review

  5. Arylethanolamines in Ritter reaction: Synthesis of 2,4‐Diarylimidazole Core

    Smorodina, A. A., Buev, E. M., Moshkin, V. S. & Sosnovskikh, V. Y., 2023, In: Asian Journal of Organic Chemistry. 12, 2, e202200656.

    Research output: Contribution to journalArticlepeer-review

  6. 2021
  7. 5-Aryloxazolidines as Reagents for Double Alkylation of Arenes: A Novel Synthesis of 4-Aryltetrahydroisoquinolines

    Buev, E. M., Smorodina, A. A., Moshkin, V. S. & Sosnovskikh, V. Y., 5 Nov 2021, In: Journal of Organic Chemistry. 86, 21, p. 15307-15317 11 p.

    Research output: Contribution to journalArticlepeer-review

  8. 2020
  9. 2019
  10. Reactions of 5-aryloxazolidines with CH-acidic compounds

    Smorodina, A. A., Buev, E. M., Moshkin, V. S. & Sosnovskikh, V. Y., 13 Jun 2019, In: Tetrahedron Letters. 60, 24, p. 1620-1623 4 p.

    Research output: Contribution to journalArticlepeer-review

  11. Nonstabilized azomethine ylides in the synthesis of aryl cucurbitine derivatives

    Buev, E. M., Smorodina, A. A., Moshkin, V. S. & Sosnovskikh, V. Y., 28 Feb 2019, In: Tetrahedron Letters. 60, 9, p. 649-652 4 p.

    Research output: Contribution to journalArticlepeer-review

  12. 2018
  13. Novel synthesis of aminoacetonitriles via the selective demethylation of quaternary ammonium salts

    Buev, E. M., Smorodina, A. A., Stepanov, M. A., Moshkin, V. S. & Sosnovskikh, V. Y., 25 Apr 2018, In: Tetrahedron Letters. 59, 17, p. 1638-1641 4 p.

    Research output: Contribution to journalArticlepeer-review

ID: 20726731